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Autor:
XENON Collaboration, Aprile, E., Aalbers, J., Abe, K., Maouloud, S. Ahmed, Althueser, L., Andrieu, B., Angelino, E., Angevaare, J. R., Antochi, V. C., Martin, D. Antón, Arneodo, F., Balata, M., Baudis, L., Baxter, A. L., Bazyk, M., Bellagamba, L., Biondi, R., Bismark, A., Brookes, E. J., Brown, A., Bruenner, S., Bruno, G., Budnik, R., Bui, T. K., Cai, C., Cardoso, J. M. R., Cassese, F., Chiarini, A., Cichon, D., Chavez, A. P. Cimental, Colijn, A. P., Conrad, J., Corrieri, R., Cuenca-García, J. J., Cussonneau, J. P., Dadoun, O., D'Andrea, V., Decowski, M. P., De Fazio, B., Di Gangi, P., Diglio, S., Disdier, J. M., Douillet, D., Eitel, K., Elykov, A., Farrell, S., Ferella, A. D., Ferrari, C., Fischer, H., Flierman, M., Form, S., Front, D., Fulgione, W., Fuselli, C., Gaemers, P., Gaior, R., Rosso, A. Gallo, Galloway, M., Gao, F., Gardner, R., Garroum, N., Glade-Beucke, R., Grandi, L., Grigat, J., Guan, H., Guerzoni, M., Guida, M., Hammann, R., Higuera, A., Hils, C., Hoetzsch, L., Hood, N. F., Howlett, J., Huhmann, C., Iacovacci, M., Iaquaniello, G., Iven, L., Itow, Y., Jakob, J., Joerg, F., Joy, A., Kara, M., Kavrigin, P., Kazama, S., Kobayashi, M., Koltman, G., Kopec, A., Kuger, F., Landsman, H., Lang, R. F., Levinson, L., Li, I., Li, S., Liang, S., Lindemann, S., Lindner, M., Liu, K., Loizeau, J., Lombardi, F., Long, J., Lopes, J. A. M., Ma, Y., Macolino, C., Mahlstedt, J., Mancuso, A., Manenti, L., Marignetti, F., Undagoitia, T. Marrodán, Martella, P., Martens, K., Masbou, J., Masson, D., Masson, E., Mastroianni, S., Mele, E., Messina, M., Michinelli, R., Miuchi, K., Molinario, A., Moriyama, S., Morå, K., Mosbacher, Y., Murra, M., Müller, J., Ni, K., Nisi, S., Oberlack, U., Orlandi, D., Othegraven, R., Paetsch, B., Palacio, J., Parlati, S., Paschos, P., Pellegrini, Q., Peres, R., Peters, C., Pienaar, J., Pierre, M., Plante, G., Pollmann, T. R., Qi, J., Qin, J., García, D. Ramírez, Rynge, M., Shi, J., Singh, R., Sanchez, L., Santos, J. M. F. dos, Sarnoff, I., Sartorelli, G., Schreiner, J., Schulte, D., Schulte, P., Eißing, H. Schulze, Schumann, M., Lavina, L. Scotto, Selvi, M., Semeria, F., Shagin, P., Shi, S., Shockley, E., Silva, M., Simgen, H., Stephen, J., Stern, M., Stillwell, B. K., Takeda, A., Tan, P. -L., Tatananni, D., Terliuk, A., Thers, D., Toschi, F., Trinchero, G., Tunnell, C., Tönnies, F., Valerius, K., Volta, G., Weinheimer, C., Weiss, M., Wenz, D., Westermann, J., Wittweg, C., Wolf, T., Wu, V. H. S., Xing, Y., Xu, D., Xu, Z., Yamashita, M., Yang, L., Ye, J., Yuan, L., Zavattini, G., Zhong, M., Zhu, T.
The multi-staged XENON program at INFN Laboratori Nazionali del Gran Sasso aims to detect dark matter with two-phase liquid xenon time projection chambers of increasing size and sensitivity. The XENONnT experiment is the latest detector in the progra
Externí odkaz:
http://arxiv.org/abs/2402.10446
Autor:
Soumah, Lucile, Desplat, Louise, Phan, Nhat-Tan, Valli, Ahmed Sidi El, Madhavan, Advait, Disdier, Florian, Auffret, Stéphane, Sousa, Ricardo, Ebels, Ursula, Talatchian, Philippe
We demonstrate the miniaturization of perpendicularly magnetized superparamagnetic tunnel junctions (SMTJs) down to 50 nm in diameter. We experimentally show stochastic reversals in those junctions, with tunable mean dwell times down to a few nanosec
Externí odkaz:
http://arxiv.org/abs/2402.03452
Autor:
Larrañaga, by J. Urrestarazu, Sisodia, Naveen, Pham, Van Tuong, Di Manici, Ilaria, Masseboeuf, Aurélien, Garello, Kevin, Disdier, Florian, Fernandez, Bruno, Wintz, Sebastian, Weigand, Markus, Belmeguenai, Mohamed, Pizzini, Stefania, Sousa, Ricardo, Buda-Prejbeanu, Liliana, Gaudin, Gilles, Boulle, Olivier
Magnetic skyrmions are topological spin textures which are envisioned as nanometre scale information carriers in magnetic memory and logic devices. The recent demonstration of room temperature stabilization of skyrmions and their current induced mani
Externí odkaz:
http://arxiv.org/abs/2308.00445
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
Creatine transporter deficiency (CTD) is an X-linked disease caused by mutations in the Slc6a8 gene. The impaired creatine uptake in the brain leads to developmental delays with intellectual disability. We hypothesized that deficient creatine uptake
Externí odkaz:
https://doaj.org/article/3bc8a604438940d7b5a62f3ce705e279
Autor:
Murra, M., Schulte, D., Cristescu, I., Disdier, J. -M., Huhmann, C., Tatananni, D., Weinheimer, C.
Publikováno v:
2022 JINST 17 P05037
Two cryogenic bath-type heat exchangers for ultra-pure noble gas applications were developed with particular emphasis on noble gas liquefaction in cryogenic distillation systems. The main objective was to construct heat exchangers for xenon from mate
Externí odkaz:
http://arxiv.org/abs/2203.01026
Autor:
Dante Culqui Lévano, Sofía Escalona López, Alín Gherasim, Jesús Oliva Domínguez, María Teresa Disdier Rico, Montserrat García Gómez
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0301344 (2024)
IntroductionDuring the COVID-19 pandemic, a set of social measures were adopted for the preservation of business activity and the protection of workers. One of these measures was issuing the Temporary Disability (TD) for COVID-19 cases, close contact
Externí odkaz:
https://doaj.org/article/c1f333f4b7d448b19664373fea59016f
Autor:
Born, Jannis, Brändle, Gabriel, Cossio, Manuel, Disdier, Marion, Goulet, Julie, Roulin, Jérémie, Wiedemann, Nina
Publikováno v:
ISMB TransMed COSI 2020
With the rapid development of COVID-19 into a global pandemic, there is an ever more urgent need for cheap, fast and reliable tools that can assist physicians in diagnosing COVID-19. Medical imaging such as CT can take a key role in complementing con
Externí odkaz:
http://arxiv.org/abs/2004.12084
Publikováno v:
BMJ Global Health, Vol 8, Iss 11 (2023)
Introduction There is a lack of quantitative evidence on the role of food innovations—new food ingredients and processing techniques—in the nutrition transition.Objective Document the distribution of food innovations across 67 high-income (HIC) a
Externí odkaz:
https://doaj.org/article/0f285ea3286f4fcca933e6d222601c3b
Autor:
Léa Broca-Brisson, Rania Harati, Clémence Disdier, Orsolya Mozner, Romane Gaston-Breton, Auriane Maïza, Narciso Costa, Anne-Cécile Guyot, Balazs Sarkadi, Agota Apati, Matthew R Skelton, Lucie Madrange, Frank Yates, Jean Armengaud, Rifat Hamoudi, Aloïse Mabondzo
Publikováno v:
eLife, Vol 12 (2023)
Creatine transporter deficiency (CTD) is an X-linked disease caused by mutations in the SLC6A8 gene. The impaired creatine uptake in the brain results in intellectual disability, behavioral disorders, language delay, and seizures. In this work, we ge
Externí odkaz:
https://doaj.org/article/e52897c931c1438dbf89ad9807783b44
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